Gastrostomy tube feeding in infancy
Symptom Information:
Symptom ID: | HPO:0011471 | ||
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abdominal symptom(HPO:0011458) Feeding difficulties(HPO:0011968) Feeding difficulties in infancy(HPO:0008872) Gastrostomy tube feeding in infancy(HPO:0011471) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
Leigh syndrome | (Orphanet:506) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |